Your browser doesn't support javascript.
loading
A Facile Design for Water-Oxidation Molecular Catalysts Precise Assembling on Photoanodes.
Jiang, Wenchao; Li, Siyuan; Sui, Qi; Gao, Yujie; Li, Fei; Xia, Lixin; Jiang, Yi.
Afiliación
  • Jiang W; College of Chemistry, Liaoning University, Shenyang, Liaoning, 110036, China.
  • Li S; School of Chemical and Materials Science, University of Science and Technology of China, Hefei, Anhui, 230026, China.
  • Sui Q; College of Chemistry, Liaoning University, Shenyang, Liaoning, 110036, China.
  • Gao Y; College of Chemistry, Liaoning University, Shenyang, Liaoning, 110036, China.
  • Li F; College of Chemistry, Liaoning University, Shenyang, Liaoning, 110036, China.
  • Xia L; State Key Laboratory of Fine Chemicals, Dalian University of Technology, Dalian, Liaoning, 116024, China.
  • Jiang Y; College of Chemistry, Liaoning University, Shenyang, Liaoning, 110036, China.
Adv Sci (Weinh) ; 11(2): e2305919, 2024 Jan.
Article en En | MEDLINE | ID: mdl-37984864
Regulating the interfacial charge transfer behavior between cocatalysts and semiconductors remains a critical challenge for attaining efficient photoelectrochemical water oxidation reactions. Herein, using bismuth vanadate (BiVO4 ) photoanode as a model, it introduces an Au binding bridge as holes transfer channels onto the surfaces of BiVO4 , and the cyano-functionalized cobalt cubane (Co4 O4 ) molecules are preferentially immobilized on the Au bridge due to the strong adsorption of cyano groups with Au nanoparticles. This orchestrated arrangement facilitates the seamless transfer of photogenerated holes from BiVO4 to Co4 O4 molecules, forming an orderly charge transfer pathway connecting the light-absorbing layer to reactive sites. An exciting photocurrent density of 5.06 mA cm-2 at 1.23 V versus the reversible hydrogen electrode (3.4 times that of BiVO4 ) is obtained by the Co4 O4 @Au(A)/BiVO4 photoanode, where the surface charge recombination is almost completely suppressed accompanied by a surface charge transfer efficiency over 95%. This work represents a promising strategy for accelerating interfacial charge transfer and achieving efficient photoelectrochemical water oxidation reaction.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Adv Sci (Weinh) Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Alemania

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Adv Sci (Weinh) Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Alemania